FDA 510(k)

女性IC（未最终确定）

K号: K213575 · 2022-09-13

决定日期2022-09-13

产品代码EZD

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决定实质等同

器械摘要

Female IC (Not Finalized) is the device name listed in this FDA 510(k) record. The listed applicant is Hollister Incorporated. It received FDA 510(k) clearance on 2022-09-13 under 510(k) number K213575. The device is classified under product code EZD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Female IC (Not Finalized)?

Female IC (Not Finalized) is a medical device that received FDA 510(k) clearance on 2022-09-13. The listed applicant is Hollister Incorporated. The 510(k) number is K213575.

When did Female IC (Not Finalized) receive FDA 510(k) clearance?

Female IC (Not Finalized) received FDA 510(k) clearance on 2022-09-13, under 510(k) number K213575.

Who is the listed applicant for Female IC (Not Finalized)?

The FDA 510(k) record lists Hollister Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Female IC (Not Finalized)?

The FDA product code for Female IC (Not Finalized) is EZD.

列明Hollister Incorporated为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

查看所有 11 个设备 →

相关器械（代码：EZD）

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K261418Liquick X-treme，Liquick X-treme PlusTeleflex Medical K260737Cure Aqua™ 即用型亲水性间歇导尿管女性用（CH06 - CH16）；Cure Aqua™ 即用型亲水性间歇导尿管男性直型（CH06 - CH18）；Cure Aqua™ 即用型亲水性间歇导尿管男性弯型（CH10 - CH18）。Convatec K261658LoFric Origo Pro CoudéWellspect AB K262045Luja软性产品Coloplast A.S.K260394一次性使用亲水性涂层间歇性纳拉通导尿管（NCR）Hangzhou Jimushi Meditech Co., Ltd.K253295Coude袖套IC；Coude Plus袖套ICHollister Incorporated

官方来源

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